NATASHA U

<ul>writing drug trial methodologies (procedures) <li>identifying and briefing appropriate trial investigators (clinicians)</li> <li>setting up and disbanding trial study centres</li> <li>designing trial materials and supplying study centres with sufficient quantities</li> <li>providing clinicians with instructions on how to conduct the trials</li> <li>collecting and authenticating data collection forms (commonly known as case report forms)</li> <li>monitoring progress throughout the duration of the trial</li> <li>writing reports</li> </ul>

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Pharmaceutical

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Clinical Research Associate

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